NDC11 43742253201
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 43742-2532-01 | 43742-2532 |
| 43742-2532-1 | 43742-2532 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| PARV Plus | ANTIMONIUM CRUDUM, APIS MELLIFICA, CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), FERRUM PHOSPHORICUM, PULSATILLA (PRATENSIS), RHUS TOX, SULPHUR, URTICA URENS | Deseret Biologicals, Inc. | 187113bf-fcec-4942-8343-dc200bd3e5e9 | 2026-01-02 | Warnings | 43742-2532-1 43742-2532 43742253201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.